NEU-LAXOVA SYNDROME - PRENATAL ULTRASONOGRAPHIC DIAGNOSIS, CLINICAL AND PATHOLOGICAL-STUDIES, AND NEW MANIFESTATIONS

被引:26
作者
SHAPIRO, I
BOROCHOWITZ, Z
DEGANI, S
DAR, H
IBSCHITZ, I
SHARF, M
机构
[1] TECHNION ISRAEL INST TECHNOL,FAC MED,BNAI ZION MED CTR,SIMON WINTER INST HUMAN GENET,POB 4940,IL-31048 HAIFA,ISRAEL
[2] TECHNION ISRAEL INST TECHNOL,FAC MED,BNAI ZION MED CTR,DEPT OBSTET & GYNECOL,HAIFA,ISRAEL
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 43卷 / 03期
关键词
NEU-LAXOVA SYNDROME; PRENATAL DIAGNOSIS; CATARACT; ULTRASONOGRAPHY; AUTOSOMAL RECESSIVE INHERITANCE; DANDY-WALKER MALFORMATION; CHOROID PLEXUS CYSTS; SCALING;
D O I
10.1002/ajmg.1320430319
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A diagnosis of the Neu-Laxova syndrome (NLS) was made by ultrasonography at 32 wks of gestation. Ultrasonographic examination showed intrauterine growth retardation (IUGR), Dandy-Walker anomaly, choroid plexus cysts, receding forehead and microcephaly, bilateral cataract without prominent eyes, scalp edema with no generalized edema, retrognathia, curved penis, and flexion deformities of limbs. The findings in this case are consistent with NLS; however, they did not fit any of Curry's [1982] groups. Massive swelling of hands and feet were among the main manifestations in classic NLS cases. In the case presented herein, edema was noted only in the scalp. This might shed further light on the question of variability vs. heterogeneity in the NLS. This case shows the existing possibility of an early diagnosis of NLS and adds Dandy-Walker anomaly and choroid plexus cysts as new findings to this syndrome.
引用
收藏
页码:602 / 605
页数:4
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